Hybrid Global Regulatory Manager – Oncology

GSK; North East; Hybrid; GBP 85,000 - 120,000; Full time

Benefits offered by this job

Annual bonus

Healthcare

Pension plan membership

Shares and savings programme

Job summary

GSK is seeking a Global Regulatory Affairs Manager for Oncology to design and execute global/regional regulatory strategies, ensuring robust labeling and timely approvals. You will work with GRL and TA Head, guiding development plans across regions with a patient-first mindset and a focus on compliant, efficient regulatory execution.

The role emphasizes collaboration in matrix teams, strong communication, and experience in oncology regulatory pathways, with a hybrid work model and access to

Qualifications

• Bachelor’s degree in biological, pharmaceutical or healthcare science.
• 1+ year of experience in drug development process, preferably in regulatory affairs and oncology.
• 1+ years of experience in clinical trial requirements in at least one major regional/global market.

Responsibilities

• Develop and execute global regulatory strategies for oncology assets.
• Collaborate with cross-functional teams to shape development plans and regulatory interactions across regions.
• Ensure labeling and approvals while maintaining compliance with internal and external requirements.
• Lead regulatory submissions and interactions with authorities.
• Drive process improvements and strategic changes in regulatory programs.
• Support interactions, reviews, and submissions with regional/local regulatory authorities.

Skills

Business Resilience

Communication

Digital Fluency

Matrix Leadership

Pharmaceutical Regulatory Compliance

Regulatory Strategies

Resource Management

Stakeholder Management

Education

Bachelor’s degree in biological, pharmaceutical or healthcare science

PhD/MD/PharmD (preferred)

Job description

GSK is seeking a Global Regulatory Affairs Manager for Oncology to design and execute global/regional regulatory strategies, ensuring robust labeling and timely approvals. You will work with GRL and TA Head, guiding development plans across regions with a patient-first mindset and a focus on compliant, efficient regulatory execution.

The role emphasizes collaboration in matrix teams, strong communication, and experience in oncology regulatory pathways, with a hybrid work model and access to